SHORT-TERM EFFECTS OF PERINATAL ASPHYXIA STUDIED WITH FOS-IMMUNOCYTOCHEMISTRY AND IN-VIVO MICRODIALYSIS IN THE RAT

被引:26
作者
DELLANNA, E
CHEN, Y
LOIDL, F
ANDERSSON, K
LUTHMAN, J
GOINY, M
RAWAL, R
LINDGREN, T
HERRERAMARSCHITZ, M
机构
[1] KAROLINSKA INST,DEPT PHYSIOL & PHARMACOL,S-17177 STOCKHOLM,SWEDEN
[2] HUDDINGE HOSP,KAROLINSKA INST,DEPT INTERNAL MED,S-14186 HUDDINGE,SWEDEN
[3] UNIV UDINE,DEPT NEUROL,UDINE,ITALY
[4] ASTRA ARCUS AB,CNS PRECLIN RES & DEV,BEHAV & BIOCHEM PHARMACOL,SODERTALJE,SWEDEN
关键词
D O I
10.1016/0014-4886(95)90050-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the present study, the short-term consequences of various perinatal asphyctic periods were studied at the peripheral and CNS levels in the rat. Perinatal asphyxia was induced in rat pups delivered by caesarean section within the last day of gestation, by placing the uterus horns including the fetuses in a water bath at 37 degrees C for various periods of time (0-23 min). Following asphyxia, the uterus horns were opened. The pups were then removed and stimulated to breathe. Subcutaneous levels of pyruvate (Pyr), lactate (Lact), glutamate (Glu), and aspartate (Asp) were monitored with microdialysis 40 min after delivery. In parallel experiments, the pups were sacrificed 80 min after delivery. The brains were removed, fixed, cut, and processed for Fos immunocytochemistry. The number of Fos-immunoreactive (IR) cells in different brain structures was counted under light microscopy. Subcutaneous levels of Pyr, Lact, Glu, and Asp increased following perinatal asphyxia, as compared to caesarean-delivered pups or to spontaneously delivered controls. A maximum increase in Pyr levels (approximate to threefoId) was observed with 2-3 min of asphyxia, while Lact levels increased along with the length of asphyxia. A maximum increase in Glu and Asp levels (approximate to threefold) was observed with 10-11 min of asphyxia. Fos-IR nuclei were predominantly found in the piriform cortex, and in the cortical amygdaloid complex. In some cases, mainly in pups exposed to asphyxia, Fos-positive cells were also seen in other tele-diencephalic structures. The number of Fos-IR cells in the piriform cortex increased following short asphyctic periods, with a maximum increment in animals exposed to 2-3 min asphyxia (approximate to twofold). In contrast, asphyctic periods longer than 10 min were associated with a decrease in the number of Fos-IR cells (>50%). A strong decrease in Fos-IR was also observed in the cortical amygdaloid complex following during recirculation in rats surviving various asphyctic periods are suggestive of diffuse stimulatory and inhibitory responses to the progressive failure in energy reserves that follows prolonged asphyxia. It is speculated that these changes may be involved in the processes leading to the behavioral alterations observed in experimental animals as well as in humans surviving perinatal asphyxia. (C) 1995 Academic Press, Inc.
引用
收藏
页码:279 / 287
页数:9
相关论文
共 44 条
[1]   EXCITATORY AMINO-ACIDS CONTRIBUTE TO THE PATHOGENESIS OF PERINATAL HYPOXIC-ISCHEMIC BRAIN INJURY [J].
BARKS, JDE ;
SILVERSTEIN, FS .
BRAIN PATHOLOGY, 1992, 2 (03) :235-243
[2]  
BAYERS SA, 1991, NEOCORTICAL DEV
[3]   ASPHYCTIC LESION - PROLIFERATION OF TYROSINE HYDROXYLASE-IMMUNOREACTIVE NERVE-CELL BODIES IN THE RAT SUBSTANTIA-NIGRA AND FUNCTIONAL-CHANGES IN DOPAMINE NEUROTRANSMISSION [J].
BJELKE, B ;
ANDERSSON, K ;
OGREN, SO ;
BOLME, P .
BRAIN RESEARCH, 1991, 543 (01) :1-9
[4]   REGIONAL EXPRESSION OF C-FOS AND HEAT-SHOCK PROTEIN-70 MESSENGER-RNA FOLLOWING HYPOXIA ISCHEMIA IN IMMATURE RAT-BRAIN [J].
BLUMENFELD, KS ;
WELSH, FA ;
HARRIS, VA ;
PESENSON, MA .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1992, 12 (06) :987-995
[5]  
CHOI DW, 1990, J NEUROSCI, V10, P2493
[6]   TRANSIENT CHANGES IN FOS AND GFAP IMMUNOREACTIVITY PRECEDE NEURONAL LOSS IN THE RAT HIPPOCAMPUS FOLLOWING NEONATAL ANOXIA [J].
DELLANNA, ME ;
GELOSO, MC ;
DRAISCI, G ;
LUTHMAN, J .
EXPERIMENTAL NEUROLOGY, 1995, 131 (01) :144-156
[7]   ATP AND BRAIN-FUNCTION [J].
ERECINSKA, M ;
SILVER, IA .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1989, 9 (01) :2-19
[8]   IMMEDIATE-EARLY GENE INDUCTION AFTER NEONATAL HYPOXIA-ISCHEMIA [J].
GUBITS, RM ;
BURKE, RE ;
CASEYMCINTOSH, G ;
BANDELE, A ;
MUNELL, F .
MOLECULAR BRAIN RESEARCH, 1993, 18 (03) :228-238
[9]   EFFECTS OF HYPOXIA-ISCHEMIA AND SEIZURES ON NEURONAL AND GLIAL-LIKE C-FOS PROTEIN-LEVELS IN THE INFANT RAT [J].
GUNN, AJ ;
DRAGUNOW, M ;
FAULL, RLM ;
GLUCKMAN, PD .
BRAIN RESEARCH, 1990, 531 (1-2) :105-116
[10]   EFFECT OF ANOXIA ON ION DISTRIBUTION IN THE BRAIN [J].
HANSEN, AJ .
PHYSIOLOGICAL REVIEWS, 1985, 65 (01) :101-148